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Evaluation for Benign and Malignant Pulmonary Ground-glass Nodules Based on MRI Dynamic Contrast Enhanced Imaging

Q

Qianfoshan Hospital

Status

Unknown

Conditions

Pulmonary Nodules

Treatments

Diagnostic Test: MRI scan

Study type

Interventional

Funder types

Other

Identifiers

NCT05067023
QianfoshanH Z

Details and patient eligibility

About

Computed tomography (CT) is critical for the diagnosis of lung nodules as well as for therapeutic management. Repeated CT examinations will raise the issue of the cumulative radiation dose and subsequent risk of cancer, thus pushing the need for imaging techniques using low or no radiation dose. Magnetic Resonance Imagery (MRI) with ultrashort echo time (UTE) pulse sequences with high signal-to-noise and spatial resolution is a promising alternative for lung nodules imaging.The purpose of the study is to evaluate the value of dynamic contrast-enhanced MR imaging (DCE-MRI) to discriminate of malignant from benign lesions.

Full description

Computed tomography (CT) is critical for the diagnosis of lung nodules as well as for therapeutic management. Repeated CT examinations will raise the issue of the cumulative radiation dose and subsequent risk of cancer, thus pushing the need for imaging techniques using low or no radiation dose. Magnetic Resonance Imagery (MRI) with ultrashort echo time (UTE) pulse sequences with high signal-to-noise and spatial resolution is a promising alternative for lung nodules imaging.The purpose of the study is to evaluate the value of DCE-MRI to discriminate of malignant from benign lesions.In this study, the investigators are going to validate the efficacy of the DCE-MRI for diagnosing early lung cancer by comparing results of the pre-surgery MRI imaging with the post-surgery pathology.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Ground-glass pulmonary nodules found by CT scan
  • Plan to accept surgery or puncture due to the pulmonary nodules
  • Absence of treatment such as chemotherapy or radiotherapy and biopsy
  • Adequate renal function to tolerate intravenous gadolinium
  • Agree to sign informed consent
  • Able to lie still during DCE-MRI

Exclusion criteria

  • Fail to understand or agree to sign informed consent
  • Implanted pacemaker or cardiac defibrillator
  • Contraindications to undergoing MRI
  • Uncontrolled intercurrent illness
  • Pregnant or breastfeeding

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

MRI scan
Experimental group
Description:
All participants will undergo 1 DCE-MRI scan before surgery or puncture.
Treatment:
Diagnostic Test: MRI scan

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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